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Usage

Uses

Used in Perfume Industry:
7-Megastigmene-3,5,6,9-tetrol is used as a fragrance ingredient for its characteristic aroma, enhancing the scent profiles of various perfumes and fragrant products.
Used in Flavor Industry:
7-Megastigmene-3,5,6,9-tetrol is used as a flavoring agent for its distinct taste, adding unique flavor notes to food and beverage products.
Used in Pharmaceutical Industry:
7-Megastigmene-3,5,6,9-tetrol is studied for its potential therapeutic properties, such as antioxidant and anti-inflammatory effects, which may contribute to the development of new pharmaceutical products for various health applications.
Used in Cosmetic Industry:
Due to its potential antioxidant and anti-inflammatory properties, 7-Megastigmene-3,5,6,9-tetrol may be utilized in cosmetic products to provide skincare benefits and enhance the overall quality of cosmetic formulations.

Relevant academic research and scientific papers

Megastigmanes from the aerial part of Euphorbia heterophylla

Three unprecedented megastigmanes together with twelve known compounds were isolated from the aerial part of Euphorbia heterophylla. The structural elucidation was based on extensive uses of spectroscopic data. The absolute configuration assignment of 1 was based on NOESY correlations and comparison of the experimental and calculated ECD spectra. Selected isolates obtained in sufficient quantity were evaluated for their cytotoxic activity.

Stereochemistry of megastigmane glucosides from Glochidion zeylanicum and Alangium premnifolium

From Glochidion zeylanicum, two megastigmane glucosides, 3- and 9-O-β-D-glucopyranosides of (3S,5R,6R,7E,9S)-megastigman-7-ene-3,5,6,9-tetrol (1 and 2, respectively), were isolated. Their structures were different from those of kiwiionoside (3) and actinidioionoside (4), isolated from Actinidia chinensis and Actinidia polygama, respectively, in the stereochemistry at the 9-positions. Alangionosides E (5) and O (6), isolated from the leaves of Alangium premnifolium, are also megastigmane glucosides, and the latter is closely related to 1 and actinidioionoside (4). However, the absolute configurations of the 9-position remained to be determined. They were analyzed to be R by means of a modified Mosher's method. Alangionoside E (5) is identical with corchoionoside A in all aspects. The name of corchoionoside A must be retained thereafter.